Pro+ Flat Deck Wide W/o X-ray

Recall Summary The Pro+ Flat Deck Wide W/O X-Ray device is being recalled in Canada due to a device compatibility issue. This is classified as a Class II recall, meaning the device could cause temporary adverse health effects or serious injury. The product was distributed across Canada.

Product

pro+ Flat Deck Wide W/O X-Ray

Reason

Device compatibility

Classification

Class II

Category

medical device recall

Country

Canada

Agency

HC-DEVICES

Recall date

2026-08-27

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b113b4b4-8c00-4f0a-ae24-a75ff6c09a99